Due to growth we have an immediate need for a Clinical Data Coordinator, based in the UK, to join our Global Data Management team at ProPharma.
This is a fully remote, entry level position with an opportunity for progression.
Please note: This is a HYBRID role (2/3 days in the office) for the duration of the probation period (3-6 months). After probation, the role is fully remote.
We have offices in Richmond, North Yorkshire OR Central London
The Clinical Data Coordinator position is responsible for providing Data Management support to ProPharma clients.
Main Responsibilities:
• Complete Data Management tasks for assigned studies under direction from the Clinical Data Manager leading the study.
• Operate according to applicable SOPs and study-specific documentation.
• Create test data for User Acceptance Testing (UAT).
• Perform and document database UAT.
• Perform SAE reconciliation.
• Perform reconciliation of third party external electronic data.
• Perform data review via listings and EDC system.
• Perform query processing to ensure data completeness and integrity.
• Perform pre-lock and data lock tasks.
• Participate in internal team meetings as required.
• Generate and review status metric reports as needed.
• File study documentation in SharePoint and TMF.
Necessary Skills and Abilities:
• Excellent oral and written communication, and interpersonal skills.
• Effective organizational and time management skills.
• Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
• Ability to exercise excellent attention to detail.
• Ability to maintain confidentiality.